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Learn about Thalassaemia

Alpha thalassaemia

This section is dedicated to alpha (α-) thalassaemia. THE MAJOR ALPHA (α-) THALASSAEMIAS ARE: HbH disease α-thalassaemia Hydrops Foetalis (=Hb Bart’s Hydrops Foetalis) Many diseases in humans are caused by abnormalities in the blood and these are categorized according to the component of the blood which is affected: white cell ...

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Non-Transfusion Dependent Thalassaemias (NTDTs) is a term used to label patients who do not need regular blood transfusions for survival but may need occasional or even frequent transfusions for defined periods of time.

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Thalassaemia cure

At present, the only available approach to curing thalassaemia is bone marrow transplantation, following specific requirements that both the donor and patient must fulfil. Gene therapy is being studied as a potential cure for some patients. Bone Marrow Transplantation Bone Marrow Transplantation (BMT) or Haematopoietic Stem Cell Transplantation (HSCT) is a ...

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Clinical Trials and updates

Clinical trials are experiments or observations carried out in clinical research, designed to answer specific questions about new treatments such as novel vaccines, drugs etc. for further study and comparison.

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Beta Thalassaemia

What is beta thalassaemia This section is dedicated to beta (β-) thalassaemia syndromes of which β-thalassaemia major, also known as Mediterranean anaemia or Cooley’s Anaemia, is the clinically most severe one. THE MAJOR BETA (β-) THALASSAEMIA SYNDROMES ARE: β-thalassaemia major β-thalassaemia intermedia HbE/β-thalassaemia Other rare thalassaemias Many diseases in humans ...

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Sickle cell disease

SCD is caused by a haemoglobin defect, known as Haemoglobin S. In SCD, the bone marrow cannot produce enough healthy red cells. The red cells produced look like sickles, are not flexible and can stick on vessels’ walls causing blood clots and preventing oxygen from reaching the body tissues.

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